Canonical Allele Identifier: CA913179759
Gene:

Linked Data

ClinVar Variation Id: 689927
ClinVar RCV Id: RCV000850780
dbSNP Id: rs1556423004

Genomic Alleles

HGVS Genome Assembly
NC_012920.1:m.5528T>C , J01415.2:m.5528T>C GRCh38